Methyl 2-(N-(4-ethoxy-4-oxobutyl)-4-methylphenylsulfonamido)benzoate
95%
- Product Code: 83263
CAS:
100627-39-2
| Molecular Weight: | 419.49 g./mol | Molecular Formula: | C₂₁H₂₅NO₆S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00666419 | |
| Melting Point: | 98-100 °C | Boiling Point: | |
| Density: | 1.24 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as an intermediate in the production of more complex molecules. Its structure, featuring both sulfonamide and ester functional groups, makes it a versatile building block for the development of pharmaceuticals, particularly in the synthesis of compounds with potential anti-inflammatory or analgesic properties. Additionally, it can be employed in the creation of specialty chemicals used in agrochemical research, aiding in the development of new pesticides or herbicides. Its specific reactivity also allows for its use in the study of chemical reactions involving sulfonamides and esters, contributing to advancements in synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,190.00 |
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| 0.250 | 10-20 days | ฿14,040.00 |
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| 1.000 | 10-20 days | ฿28,080.00 |
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Methyl 2-(N-(4-ethoxy-4-oxobutyl)-4-methylphenylsulfonamido)benzoate
This compound is primarily utilized in the field of organic synthesis, where it serves as an intermediate in the production of more complex molecules. Its structure, featuring both sulfonamide and ester functional groups, makes it a versatile building block for the development of pharmaceuticals, particularly in the synthesis of compounds with potential anti-inflammatory or analgesic properties. Additionally, it can be employed in the creation of specialty chemicals used in agrochemical research, aiding in the development of new pesticides or herbicides. Its specific reactivity also allows for its use in the study of chemical reactions involving sulfonamides and esters, contributing to advancements in synthetic methodologies.
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